QA Associate Validation

Full Time
$70000 - $80000 per annum
May 6th, 2024
Braeside, Victoria, Australia
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About the role:
  • Pharmaceutical Organisation manufacturing therapeutic goods for the Australian and international markets.
  • Full-time permanent position
  • Based at their state-of-the-art facility in SE suburbs.
  • Great work culture and commitment to supporting its people.
  • Mon to Friday with standard working hours.
About your duties:
The primary role of the Validation Associate is to ensure that production and cleaning processes, systems and equipment are maintained in a validated state. This is mainly a desk-based role.
Your duties will include and are not limited to the following:
  • Preparation of process validation protocols for new formulations and scale ups.
  • Preparation of process validation protocols for manufacturing method changes when required.
  • Liaison with production to ensure process validation scheduling and completion of validation documents.
  • Organising documentation for scheduled revalidations for product processes.
  • Organising documentation in folders and maintaining the validation database for process validation.
  • Reporting of outcomes or issues to the Quality Systems Manager.
  • Preparation of Regulatory Process Validation Reports
  • Maintaining the Cleaning Validation Schedule.
  • Ensuring the correct preparation of Cleaning Validation Protocols for each cleaning event requiring validation.
  • Conducting cleaning visual assessments, validation swabbing and analytical testing when required.
  • Preparation of Cleaning Validation Reports, testing methods and sampling protocols.
  • Maintaining the cleaning validation schedule.
About you:
  • Bachelor’s degree in chemistry, Chemical Engineering or closely related discipline
  • Demonstrated experience in a laboratory environment with analytical testing OR demonstrated experience in pharmaceutical manufacturing / engineering (highly regarded)
  • Understanding of validation processes (cleaning and process)
  • Sound computer skills.
  • Thorough and diligent
  • Proactive approach to work and CAN-DO attitude
  • Excellent communication skills
If you come with relevant laboratory / manufacturing experience and have an interest in making a career change to validation you are encouraged to apply – full training provided!

If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).  
Or, if you have any questions, please contact Priyanka or Cathy on 03 9040 1630.

With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

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